ClinVar Miner

Submissions for variant NM_032609.3(COX4I2):c.1-6C>T

dbSNP: rs201853480
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000997763 SCV000714289 likely benign not provided 2018-05-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000997763 SCV001153454 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing COX4I2: BP4, BS2

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